A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496740



Internal ID20869943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45916758..46061242hg38UCSC Ensembl
chr15:46208956..46353440hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38144485
hg19144485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024640
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496740
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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